Vahabi Arman, Kaya Hüseyin, Kerekulov Bakıt, Biçer Ahmet, Keçeci Burçin, Sabah Dündar
Department of Orthopedics and Traumatology, Ege University School of Medicine, Izmir, Turkey.
Department of Orthopaedics and Traumatology, EMOT Hospital, Izmir, Turkey.
Clin Orthop Relat Res. 2025 Jun 26. doi: 10.1097/CORR.0000000000003599.
Extracorporeally irradiated autografting is a recognized technique in reconstruction after intercalary resections, but it has drawbacks such as nonunion and graft fracture. Because sterilized autografts lose some of their mechanical properties due to involvement of the cortex with tumor, the curettage, and the adverse effects of irradiation or other sterilization techniques, some have proposed adding vascularized fibula to augment the autograft. Because this potentially adds morbidity, we sought to address the value of adding vascular fibular grafts to reconstruction with irradiated autografts.
QUESTIONS/PURPOSES: Comparing patients who received an extracorporeally radiated autograft alone with those who received such a graft augmented by a free vascularized fibular autograft: (1) Was the proportion of patients who did not achieve union by 12 months higher in the group that received the augmented (vascularized) graft? (2) Did the augmented-graft group demonstrate greater survivorship free from graft loss at 72 months than did the group receiving an irradiated graft alone? (3) Were there between-group differences in functional results? (4) Were there between-group differences in complications, defined as those substantial enough to result in further surgery?
In our single-center study, conducted in a tertiary academic referral center, we performed a retrospective chart audit of patients undergoing intercalary resections for primary sarcomas of the femur and tibia. Between January 2002 and April 2023, three surgeons (HK, BK, DS) treated 345 patients for bone sarcoma of the femur or tibia. Of those, we considered 25% (85) treated with intercalary resection for primary bone sarcomas as potentially eligible. A further 7% (23 of 345) of patients were excluded because their reconstruction was performed using a technique other than irradiated autografts. Another 2% (6) had died prior to the minimum follow-up period of 24 months, another 1% (3) did not finish the 24-month follow-up, and 1% (3) were lost to follow-up for > 5 years, leaving 14% (50 of 345) for analysis here. Among these, 26% (13 of 50) of patients underwent reconstruction involving an extracorporeally irradiated autograft and augmentation with a vascularized fibula autograft. In the remaining 37 patients, reconstruction was performed using extracorporeally irradiated bone alone. During this period, intercalary resection was typically indicated for patients with primary bone sarcomas located in the metaphyseal or diaphyseal regions without articular involvement, provided that they demonstrated a favorable response to neoadjuvant therapy. In this predominantly young patient cohort, extracorporeally irradiated autografts were our preferred reconstruction method after sarcoma resection. Isolated extracorporeally irradiated autografts were selected for patients with radiologic evidence of adequate bone quality and preserved cortical integrity. In patients who have a tumor with extensive cortical destruction-yet still considered suitable for reconstruction after irradiation-vascularized fibular grafts were added to the irradiated autografts. In the group reconstructed with irradiated autograft alone, 54% (20 of 37) of patients were male and 46% (17) were female, with a median (range) age of 15 years (4 to 60). The diagnoses included osteosarcoma in 51% (19 of 37) of patients and Ewing sarcoma in 32% (12). The tumor was located in the tibia in 59% (22) of patients and in the femur in 41% (15). In the group receiving irradiated autograft augmented with vascularized fibula, 6 of the 13 patients were male and 7 were female, with a median (range) age of 13 years (6 to 40). Diagnoses included osteosarcoma in eight of 13 patients, Ewing sarcoma in four, and malignant mesenchymal tumor in one patient. Tumor originated from the femur in 11 patients and from the tibia in two. The two groups were similar in terms of histopathologic diagnosis, age, gender, follow-up duration, and tumor location within bone while the proportion of tumors originating from the femur was higher in the group treated with vascularized fibula augmentation (85% versus 41%; p < 0.05). Fixation technique, the ratio of the resected bone length to the entire bone, was noted using the first postoperative radiograph. Bony union, defined as bony bridging in at least three cortices, was assessed using two-plane radiographs. Patients who achieved bony union within the first 12 months without undergoing any additional surgical intervention were classified as having union. Patients whose autograft incorporation exceeded 12 months but ultimately achieved union before 15 months without the need for additional intervention were classified as having delayed union. Nonunion was defined as when patients demonstrated incomplete integration at the 15-month follow-up or when patients needed additional intervention before healing. The survival of extracorporeally irradiated autografts, free from any degree of loss (partial or complete graft loss attributed to graft fracture resorption or graft removal after infection or recurrence), was assessed using competing risk analysis, with death as a competing event at 72 months postoperatively. Functional outcomes were measured using the 1993 version of the Musculoskeletal Tumor Society (MSTS) scoring system with its six subheadings. Complications were defined as events that were substantial enough to result in surgery. Problems related to fibular donor site were also recorded.
In patients who received reconstruction with irradiated autografts alone, graft loss occurred in five patients before union was achieved, and one patient died before 12 months; thus, these patients were excluded from analysis on union within 12 months. Among the remaining 31 patients, union was achieved within 12 months in 71% (22) of patients, delayed union in 16% (5) of patients, and nonunion in 13% (4) of patients. In the group in which vascularized fibula was used to augment the irradiated autograft, union occurred within 12 months in 9 of 13 patients, while delayed union and nonunion were observed in two patients each. There was no difference between the groups (p > 0.99). At 72 months, the cumulative incidence of graft loss was 32% (95% confidence interval [CI] 19.1% to 47.6%) in the irradiated autograft-alone group and 13% (95% CI 2.3% to 40.3%) in the fibula-augmented group. The cumulative incidence of death at 72 months was 25% (95% CI 13.9% to 40.3%) in the irradiated autograft-alone group and 20% (95% CI 5.0% to 48.6%) in the fibula-augmented group. Competing risk regression for graft loss, treating death as a competing event, showed no difference between the groups (subdistribution HR 0.42 [95% CI 0.10 to 1.84]; p = 0.25). The median (range) MSTS score in patients reconstructed with irradiated autograft alone was 27 (18 to 30), while the median (range) MSTS score in those reconstructed with irradiated autograft augmented with vascularized fibula was 24 (20 to 30), and there were no differences between the groups in terms of total MSTS scores or any of the MSTS subdomains. In patients reconstructed with irradiated autograft alone, a total of 28 complications were observed in 20 patients. For those patients, the median (range) time from surgery to complication was 15 months (2 to 72). In patients reconstructed with irradiated autograft augmented with vascularized fibula, a total of nine complications were observed in seven patients. For those patients, the median (range) time from surgery to occurrence of complication was 18 months (1 to 23). There was no difference between the two groups in terms of the proportion of patients who faced complication or the median time to occurrence of complications. A total of four patients experienced donor site-related problems, none of which resulted in further surgery.
Despite being applied in tougher lesions with less favorable bone quality, the addition of a vascularized fibula into extracorporeally irradiated autograft for reconstruction of intercalary resections yielded comparable outcomes in terms of bony union, graft survival, functional scores, and complications when compared with patients with more favorable host bone who received reconstruction with irradiated graft alone. Although our numbers were small, given the complexity and additional morbidity associated with vascularized fibular graft, its use might be reserved for selected patients in whom biological reconstruction is desired, but the host bone is deemed weakened and unlikely to be successful compared with those patients with more intact bone. Larger studies comparing this technique with other reconstruction options such as structural allografts, intercalary endoprostheses, or cement-rod constructs are needed to better define its role. We recommend reserving the use of vascularized fibula augmentation as a reinforcement strategy in reconstructions with irradiated autografts after intercalary resections of the femur and tibia, opting for it only when additional benefit is anticipated, given that it prolongs operative time, necessitates the involvement of a reconstructive surgery team, and introduces additional donor-site considerations.
Level III, therapeutic study.
体外照射自体骨移植是节段性切除术后重建的一种公认技术,但存在诸如骨不连和移植骨骨折等缺点。由于灭菌后的自体骨因皮质受累于肿瘤、刮除以及照射或其他灭菌技术的不良影响而失去了一些力学性能,一些人建议添加带血管腓骨以增强自体骨。由于这可能会增加发病率,我们试图探讨在照射自体骨重建中添加带血管腓骨移植的价值。
问题/目的:比较单纯接受体外照射自体骨移植的患者与接受带血管游离腓骨自体骨增强移植的患者:(1)在接受增强(带血管)移植的组中,12个月时未实现骨愈合的患者比例是否更高?(2)增强移植组在72个月时的移植骨无丢失生存率是否高于单纯接受照射移植的组?(3)功能结果在组间是否存在差异?(4)并发症(定义为严重到足以导致进一步手术的情况)在组间是否存在差异?
在我们于三级学术转诊中心进行的单中心研究中,我们对接受股骨和胫骨原发性肉瘤节段性切除的患者进行了回顾性病历审核。2002年1月至2023年4月期间,三位外科医生(HK、BK、DS)治疗了345例股骨或胫骨骨肉瘤患者。其中,我们认为25%(85例)接受原发性骨肉瘤节段性切除治疗的患者可能符合条件。另外7%(345例中的23例)患者被排除,因为他们的重建采用了除照射自体骨移植以外的技术。另有2%(6例)在最短24个月的随访期之前死亡,1%(3例)未完成24个月的随访,1%(3例)失访超过5年,在此留下14%(345例中的50例)用于此处分析。其中,26%(50例中的13例)患者接受了涉及体外照射自体骨移植并用带血管腓骨自体骨增强的重建。在其余37例患者中,仅使用体外照射骨进行重建。在此期间,节段性切除通常适用于位于干骺端或骨干区域且无关节受累的原发性骨肉瘤患者,前提是他们对新辅助治疗显示出良好反应。在这个以年轻患者为主的队列中,体外照射自体骨移植是我们肉瘤切除术后首选的重建方法。对于骨质量足够且皮质完整性保留的患者,选择单纯体外照射自体骨移植。对于肿瘤伴有广泛皮质破坏但仍被认为适合照射后重建的患者,在照射自体骨移植中添加带血管腓骨移植。在仅用照射自体骨重建的组中,54%(37例中的20例)患者为男性,46%(17例)为女性,中位(范围)年龄为15岁(4至60岁)。诊断包括骨肉瘤51%(37例中的19例)、尤因肉瘤32%(12例)。肿瘤位于胫骨59%(22例)患者、位于股骨41%(15例)患者。在接受带血管腓骨增强照射自体骨移植的组中,13例患者中有6例为男性,7例为女性,中位(范围)年龄为13岁(6至40岁)。诊断包括13例患者中的8例骨肉瘤、4例尤因肉瘤和1例恶性间叶肿瘤患者。肿瘤起源于股骨11例患者、起源于胫骨2例患者。两组在组织病理学诊断、年龄、性别、随访时间以及骨内肿瘤位置方面相似,而带血管腓骨增强治疗组中起源于股骨的肿瘤比例更高(85%对41%;p < 0.05)。使用术后第一张X线片记录固定技术,即切除骨长度与整个骨的比例。骨愈合定义为至少三个皮质出现骨桥接,使用双平面X线片进行评估。在12个月内实现骨愈合且未接受任何额外手术干预的患者被分类为已愈合。自体骨融合超过12个月但最终在15个月前无需额外干预而实现愈合的患者被分类为延迟愈合。骨不连定义为患者在15个月随访时显示不完全融合或在愈合前需要额外干预。使用竞争风险分析评估体外照射自体骨移植的生存率,无任何程度的丢失(部分或完全移植骨丢失归因于移植骨骨折吸收或感染或复发后移植骨移除),将死亡作为术后72个月的竞争事件。使用1993年版肌肉骨骼肿瘤学会(MSTS)评分系统及其六个子标题测量功能结果。并发症定义为严重到足以导致手术的事件。还记录了与腓骨供区相关的问题。
在仅接受照射自体骨移植重建的患者中,5例患者在实现骨愈合前发生移植骨丢失,1例患者在12个月前死亡;因此,这些患者被排除在12个月内骨愈合分析之外。在其余31例患者中,71%(22例)患者在12个月内实现骨愈合,16%(5例)患者延迟愈合,13%(4例)患者骨不连。在使用带血管腓骨增强照射自体骨移植的组中,13例患者中有9例在12个月内实现骨愈合,2例患者出现延迟愈合和骨不连。两组之间无差异(p > 0.99)。在72个月时,单纯照射自体骨移植组的移植骨丢失累积发生率为32%(95%置信区间[CI] 19.1%至47.6%),腓骨增强组为13%(95% CI 2.3%至40.3%)。72个月时的死亡累积发生率在单纯照射自体骨移植组为25%(95% CI 13.9%至40.3%),在腓骨增强组为20%(95% CI 5.0%至48.6%)。将死亡作为竞争事件的移植骨丢失竞争风险回归显示两组之间无差异(亚分布风险比0.42 [95% CI 0.10至1.84];p = 0.25)。仅用照射自体骨重建的患者的中位(范围)MSTS评分为27(从18至30),而用带血管腓骨增强照射自体骨重建的患者的中位(范围)MSTS评分为24(从20至30),两组在总MSTS评分或任何MSTS子域方面无差异。在仅用照射自体骨重建的患者中,20例患者共观察到28例并发症。对于这些患者,从手术到并发症的中位(范围)时间为15个月(从2至72)。在接受带血管腓骨增强照射自体骨移植的患者中,7例患者共观察到9例并发症。对于这些患者,从手术到并发症发生的中位(范围)时间为18个月(从1至23)。两组在面临并发症的患者比例或并发症发生的中位时间方面无差异。共有4例患者出现供区相关问题,均未导致进一步手术。
尽管在骨质量较差的更具挑战性的病变中应用,但在体外照射自体骨移植中添加带血管腓骨用于节段性切除重建,与接受单纯照射移植的宿主骨条件较好的患者相比,在骨愈合、移植骨存活、功能评分和并发症方面产生了可比的结果。尽管我们的数据量较小,但鉴于带血管腓骨移植的复杂性和额外发病率,其使用可能仅限于那些希望进行生物重建但宿主骨被认为较弱且与骨更完整的患者相比不太可能成功的特定患者。需要进行更大规模的研究,将该技术与其他重建选择如结构性同种异体骨、节段性假体或骨水泥棒结构进行比较,以更好地确定其作用。我们建议在股骨和胫骨节段性切除后用照射自体骨重建中,将带血管腓骨增强作为一种强化策略,仅在预期有额外益处时选择使用,因为它会延长手术时间,需要重建手术团队参与,并引入额外的供区考虑因素。
III级,治疗性研究。